Screening for Plasminogen Mutations in Hereditary Angioedema Patients

Hereditary angioedema (HAE) is a rare disease belonging to the group of bradykinin-mediated angioedemas, characterized by recurring edematous episodes involving the subcutaneous and/or submucosal tissues. Most cases of HAE are caused by mutations in the SERPING1 gene encoding C1-inhibitor (C1-INH-HA...

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Detalles Bibliográficos
Autores principales: Farkas, Henriette, Dóczy, Anna, Szabó, Edina, Varga, Lilian, Csuka, Dorottya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998782/
https://www.ncbi.nlm.nih.gov/pubmed/33799813
http://dx.doi.org/10.3390/genes12030402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998782/
https://www.ncbi.nlm.nih.gov/pubmed/33799813
http://dx.doi.org/10.3390/genes12030402

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